Canonical Allele Identifier: PA2825497210
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2763896
ClinVar RCV Id: RCV003503317

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077072.1:p.Leu1137Pro
CA374111724
NM_001083603.3:c.3410T>C