Canonical Allele Identifier: PA071606
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 221931

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000255.2:p.Thr1064Met
CA071573
NM_000264.5:c.3191C>T