Canonical Allele Identifier: PA2825122048
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3231012
ClinVar RCV Id: RCV004523126

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000255.2:p.Val1131Leu
CA374111764
NM_000264.5:c.3391G>T
CA374111765
NM_000264.5:c.3391G>C