Canonical Allele Identifier: PA2825487266
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 823625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077071.1:p.Arg1047Cys
CA5138167
NM_001083602.3:c.3139C>T